Archive: 2025/11

Bioequivalent medications are generic drugs proven to work the same as brand-name versions in your body. Learn how the FDA tests for equivalence, why it matters, and when to ask questions.

Tirzepatide (Zepbound) is a dual incretin therapy that targets GLP-1 and GIP receptors for significant weight loss. Learn how it works, what to expect, side effects, cost, and real results from clinical trials and patient experiences.

Five practical, evidence-based medication safety tips for seniors and caregivers to prevent dangerous drug interactions, missed doses, and hospitalizations. Backed by the FDA and geriatric experts.

Losing even 5-7% of your body weight can dramatically improve blood sugar control and even reverse type 2 diabetes. Discover science-backed strategies for safe, sustainable weight loss that work with diabetes.

The FDA now enforces strict, unannounced inspections on foreign generic drug factories to ensure safety. Learn how CGMP standards, inspection gaps, and new policies are reshaping global drug manufacturing for American patients.

Levothyroxine is effective for hypothyroidism, but safety depends on proper dosing and regular TSH monitoring. Brand switches, missed tests, and poor timing can cause serious side effects. Know how to protect yourself.

Survivorship care plans guide cancer survivors through post-treatment follow-up, screening for late effects, and healthy living. Learn what’s included, why it matters, and how to get one-even if your hospital doesn’t offer it.

Generic drug exclusivity periods vary widely across countries, affecting drug prices and access. Learn how the U.S., EU, Canada, and others regulate generic entry and why these rules matter for patients and healthcare systems.

The FDA's 2025 update to biosimilar approval rules removes outdated clinical trial requirements, speeding up access to lower-cost biologic alternatives for cancer, arthritis, and other chronic conditions.

Stability testing ensures generic drugs remain safe and effective over time. The FDA requires rigorous testing of three batches under real and accelerated conditions to prove shelf life, potency, and purity match brand-name drugs.